Tag | Content |
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EnhancerAtlas ID | HS059-02362 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr1:110779850-110781180 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxd3 | MA0041.1 | chr1:110779925-110779937 | AAACAAACATTT | - | 6.27 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65653 | chr1:110780194-110781093 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 2 | ID | Chromosome | Start | End |
GH01I110237 | chr1 | 110780195 | 110781093 | GH01I110238 | chr1 | 110781136 | 110781931 |
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Enhancer Sequence | AGGAGGTTGA GGCTGCAGTG AGCTATGATC ATACCACTGC ACTCCAGCCT GGGCGACAGA 60 ACGAGACCCT GTCTCAAACA AACATTTATT TAATACAAGG TATTGGAAAC CATCCCCATA 120 CCAAATCAAC AGGGAATCCC CTGTCACCCT TCCTCAGTCC CACTTTCCTC CCCAGAGGTG 180 ACATGGTTAA CATCTGGTGT GGGTCCTCCC AGGCTTTTTG GAAAAAAAAA AAACTTTCTA 240 ACAAAATTAC CAAATCAAAA TGGGTTTCCC TGCGGGGTAG TGAAGTTCCC TTCCCTGAAA 300 ATGTTTGGAG ACACAGTGGA TGATCATGTG CTGCACCAGG GTTCGTGGGA AGTATTTCTG 360 CTCGGCGTGG GAGGTGGAAT TAGAAGACTG TTTCCAATCC TAAGACTTTC TGACTCACGT 420 GGCACACACA GCTAGTTAGT GGTGGAGGCA GGTCCAGAAC ACAGGTATTC AGATGGGGTT 480 CAGATGAACT CCTTTCCTAG CAAGATTTTC CTTAAATTCT TCTCTGCCTC TTCCCAGCCC 540 ATCAGGGATA TAGGGCAGGG CAGAGAGACA TCTGTGTCTC CTCTAGTCTG GAGCGAGGGG 600 AGTGTCCTGG GCCTGGGTTG TGATGCCATC CAGTGCCCAC CCTCGTGGGG CTCCTGTGGC 660 ATTATTGCAG TGAGCACTTT CTTTCCGTTC CTGGCTCCAA GCCCTGTGTG TGCATACACT 720 GGTACCCACA CAAGAGGTAG CACGTGAGCT GGCTCAGTCA CTTGGGGCTG TGGTAACCGC 780 ATTCAAAATG CAGCATCATG CTAAAGAGCC GCTGGGGACT CTGGGGACAA GGCTGTCTCC 840 GACCCAGCTT TAGGGGGTGA GGAGAGGGAG CCAAACGGCT ACAGCTGCAA GTCAAAGAGG 900 TCAGAGGCCT TCTGATGTTG GCACTGGAAG CCTCTCCTTT CTTTCCCCAC AGGTTATGGG 960 GGCTTCTCCA CTCCCCGCTC TTACTTGCCT GCTTCTCCAG GGATCCCTAG AAGAGCAGTG 1020 GTTAGCAAGC ATATGCTATA GCCATCAAAT ACGAGTCTAC AGAAATGTAG GCTTCCCCTT 1080 GGGGCTGAGT TAGGGCCTCT GCTTCTGAAA TGAGCAACCT CTGGTTGCTG GTGGGGGCTA 1140 GGGCTTGCTC CCTTTCTCTC CTCACATACT CTTTCCTGGG TGACCTCATC CCCTCCCATT 1200 GCCTTAAACA TCTTCCAGGT ACTGGTGTCA TCCACTTGTG TAGTTCCAGT TCAGAAATCC 1260 CGTCAGCTCC ATTCATTCAT TTGTTCATTC ATTCAGCAAA CATATGTGGC ATCTCTGTCC 1320 CAGGTACTGC 1330
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